Abstract
Treatment of N-propionylaminoindine with a solution of phosgene in benzene gives the 1-[(indolin-1-yl)imino]propyl ester of 7-(1-cyanoethyl)indoline-1-carboxylic acid. The structure of the compound was proved using1H and13C NMR spectroscopy.
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References
N. V. Shorina, G. A. Golubeva, L. A. Svirodova, and V. N. Torocheshnikov, Khim. Geterotsikl. Soedin., No. 3, 337 (1990).
N. V. Shorina, G. A. Golubeva, L. A. Svirodova, V. N. Torocheshnikov, and A. V. Sadovoi, Khim. Geterosikl. Soedin., No. 9, 1185 (1990).
V. P. Zhestkov and Yu. N. Portnov, The Chemistry, Biochemistry and Pharmacology of Indoles, Second All Soviet Conference [in Russian], Tbilisi (1991), p. 79.
N. V. Shorina, G. A. Golubeva, L. A. Svirodova, and V. N. Torocheshnikov, Khim. Geterosikl. Soedin., No. 3, 332 (1990).
V. P. Zhestkov, V. N. Barinova, Yu. N. Portnov, and A. I. Chernyshev, Bulletin of the All-Russian Science Center for the Safety of Biologically Active Materials [in Russian], No. 2, p. 52 (1993).
Additional information
All-Russian Science Center for the Safety of Biologically Active Materials, Staraya Kupavna, Moscow Region 142450. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 168–170, February, 1995. Original article submitted January 11, 1995.
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Zhestkov, V.P., Barinova, V.N., Portnov, Y.N. et al. Heterocyclization of N-propionylaminoindoline. Chem Heterocycl Compd 31, 144–145 (1995). https://doi.org/10.1007/BF01169668
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DOI: https://doi.org/10.1007/BF01169668